• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

细胞色素P450 3A基因家族在胃癌中的作用:揭示个性化治疗的诊断生物标志物和治疗靶点。

Cytochrome P450 3A gene family in gastric cancer: Unveiling diagnostic biomarkers and therapeutic targets for personalized treatment.

作者信息

Zhu Jun-Kun, Wang Jing

机构信息

Department of Medicine, The Chinese University of Hong Kong, Hong Kong 999077, China.

The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou 510120, Guangdong Province, China.

出版信息

World J Clin Oncol. 2025 Apr 24;16(4):101548. doi: 10.5306/wjco.v16.i4.101548.

DOI:10.5306/wjco.v16.i4.101548
PMID:40290702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12019269/
Abstract

The cytochrome P450 3A () gene family's role in early progression of gastric cancer was comprehensively investigated. Its potential as a therapeutic target was evaluated. Upon literature review, aberrant expression of the gene family has a strong correlation with gastric cancer onset, although the precise underlying mechanisms remain unclear. To assess its potential as a biomarker for early diagnosis and a therapeutic target, we have provided a comprehensive review of the regulatory mechanisms governing gene family expression in gastric cancer, as well as its relation with early tumor progression and the tumor microenvironment. The gene family is crucial in the proliferation, migration, and invasion of gastric cancer cells and promotes cancer progression by modulating inflammatory responses and oxidative stress within the tumor microenvironment. Furthermore, genetic polymorphisms in enzymes highlight its potential value in personalized medicine. Based on these findings, this paper explores the feasibility of developing inhibitors and activators targeting enzymes and discusses potential applications in gene therapy. This research provides crucial theoretical support for the gene family as an early diagnostic marker and therapeutic target for gastric cancer. In the future, multi-omics studies and large-scale clinical trials will be essential to advance clinical translation of these findings.

摘要

细胞色素P450 3A()基因家族在胃癌早期进展中的作用得到了全面研究。评估了其作为治疗靶点的潜力。经文献综述,该基因家族的异常表达与胃癌发病密切相关,尽管确切的潜在机制尚不清楚。为了评估其作为早期诊断生物标志物和治疗靶点的潜力,我们全面综述了胃癌中该基因家族表达的调控机制,以及其与肿瘤早期进展和肿瘤微环境的关系。该基因家族在胃癌细胞的增殖、迁移和侵袭中起关键作用,并通过调节肿瘤微环境中的炎症反应和氧化应激促进癌症进展。此外,酶的基因多态性凸显了其在个性化医疗中的潜在价值。基于这些发现,本文探讨了开发靶向该酶的抑制剂和激活剂的可行性,并讨论了在基因治疗中的潜在应用。本研究为该基因家族作为胃癌的早期诊断标志物和治疗靶点提供了关键的理论支持。未来,多组学研究和大规模临床试验对于推进这些发现的临床转化至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4982/12019269/b96e8293a3b8/101548-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4982/12019269/b96e8293a3b8/101548-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4982/12019269/b96e8293a3b8/101548-g001.jpg

相似文献

1
Cytochrome P450 3A gene family in gastric cancer: Unveiling diagnostic biomarkers and therapeutic targets for personalized treatment.细胞色素P450 3A基因家族在胃癌中的作用:揭示个性化治疗的诊断生物标志物和治疗靶点。
World J Clin Oncol. 2025 Apr 24;16(4):101548. doi: 10.5306/wjco.v16.i4.101548.
2
Research progress regarding gene family in gastric cancer.胃癌相关基因家族的研究进展。
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2023 Dec 28;48(12):1874-1881. doi: 10.11817/j.issn.1672-7347.2023.230150.
3
Relevance of plasma lenvatinib concentrations and endogenous urinary cytochrome P450 3A activity biomarkers in clinical practice.血浆仑伐替尼浓度与内源性尿细胞色素 P4503A 活性生物标志物在临床实践中的相关性。
Pharmacol Res Perspect. 2024 Aug;12(4):e1241. doi: 10.1002/prp2.1241.
4
Effects of Strong Inhibition of Cytochrome P450 3A and UDP glucuronosyltransferase 1A9 and Strong Induction of Cytochrome P450 3A on the Pharmacokinetics, Safety, and Tolerability of Soticlestat: Two Drug-Drug Interaction Studies in Healthy Volunteers.细胞色素P450 3A和尿苷二磷酸葡萄糖醛酸基转移酶1A9的强效抑制及细胞色素P450 3A的强效诱导对索替司他药代动力学、安全性和耐受性的影响:两项在健康志愿者中的药物相互作用研究
Drug Metab Dispos. 2024 Feb 14;52(3):180-187. doi: 10.1124/dmd.123.001444.
5
Identification, characterization, and ontogeny of a second cytochrome P450 3A gene from the fresh water teleost medaka (Oryzias latipes).从淡水硬骨鱼青鳉(Oryzias latipes)中鉴定、表征及研究第二种细胞色素P450 3A基因的个体发生。
Mol Reprod Dev. 2001 Feb;58(2):149-58. doi: 10.1002/1098-2795(200102)58:2<149::AID-MRD3>3.0.CO;2-X.
6
Insights into oral bioavailability enhancement of therapeutic herbal constituents by cytochrome P450 3A inhibition.通过细胞色素 P450 3A 抑制来深入了解治疗性草药成分的口服生物利用度增强。
Drug Metab Rev. 2021 Nov;53(4):491-507. doi: 10.1080/03602532.2021.1917598. Epub 2021 Apr 27.
7
Cytochrome P450 3A, NADPH cytochrome P450 reductase and cytochrome b5 in the upper airways in horse.马的上呼吸道中的细胞色素P450 3A、NADPH细胞色素P450还原酶和细胞色素b5。
Res Vet Sci. 2008 Aug;85(1):80-5. doi: 10.1016/j.rvsc.2007.09.012. Epub 2007 Nov 5.
8
Xyloketal B, a marine compound, acts on a network of molecular proteins and regulates the activity and expression of rat cytochrome P450 3a: a bioinformatic and animal study.木酮糖酮B,一种海洋化合物,作用于分子蛋白网络并调节大鼠细胞色素P450 3a的活性和表达:一项生物信息学和动物研究。
Drug Des Devel Ther. 2014 Dec 12;8:2555-602. doi: 10.2147/DDDT.S73476. eCollection 2014.
9
CXC chemokine receptor 4 - mediated immune modulation and tumor microenvironment heterogeneity in gastric cancer: Utilizing multi-omics approaches to identify potential therapeutic targets.CXC趋化因子受体4介导的胃癌免疫调节及肿瘤微环境异质性:利用多组学方法鉴定潜在治疗靶点
Biofactors. 2025 Jan-Feb;51(1):e2130. doi: 10.1002/biof.2130. Epub 2024 Oct 21.
10
Midazolam metabolism in cytochrome P450 3A knockout mice can be attributed to up-regulated CYP2C enzymes.细胞色素P450 3A基因敲除小鼠中咪达唑仑的代谢可归因于CYP2C酶的上调。
Mol Pharmacol. 2008 Mar;73(3):1029-36. doi: 10.1124/mol.107.043869. Epub 2007 Dec 21.

本文引用的文献

1
CYP3A4 and CYP3A5: the crucial roles in clinical drug metabolism and the significant implications of genetic polymorphisms.细胞色素P450 3A4和细胞色素P450 3A5:在临床药物代谢中的关键作用及基因多态性的重要意义
PeerJ. 2024 Dec 5;12:e18636. doi: 10.7717/peerj.18636. eCollection 2024.
2
Interaction between tacrolimus and calcium channel blockers based on CYP3A5 genotype in Chinese renal transplant recipients.中国肾移植受者中基于CYP3A5基因分型的他克莫司与钙通道阻滞剂之间的相互作用
Front Pharmacol. 2024 Aug 29;15:1458838. doi: 10.3389/fphar.2024.1458838. eCollection 2024.
3
Effect of CYP3A5 Gene Polymorphisms on Tacrolimus Blood Concentrations and Adverse Events in Allogeneic Hematopoietic Stem Cell Transplant Patients.
CYP3A5 基因多态性对异基因造血干细胞移植患者他克莫司血药浓度及不良事件的影响。
Transplant Proc. 2024 Sep;56(7):1678-1682. doi: 10.1016/j.transproceed.2024.08.012. Epub 2024 Aug 14.
4
siRNA-based therapy for gastric adenocarcinoma: what's next step?基于 siRNA 的胃腺癌治疗:下一步是什么?
Pathol Res Pract. 2024 Jun;258:155328. doi: 10.1016/j.prp.2024.155328. Epub 2024 Apr 23.
5
Research progress regarding gene family in gastric cancer.胃癌相关基因家族的研究进展。
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2023 Dec 28;48(12):1874-1881. doi: 10.11817/j.issn.1672-7347.2023.230150.
6
Identification and validation of an individualized metabolic prognostic signature for predicting the biochemical recurrence of prostate cancer based on the immune microenvironment.基于免疫微环境鉴定和验证用于预测前列腺癌生化复发的个体化代谢预后特征。
Eur J Med Res. 2024 Jan 31;29(1):92. doi: 10.1186/s40001-024-01672-3.
7
Association of systemic inflammatory markers and tertiary lymphoid structure with pathological complete response in gastric cancer patients receiving preoperative treatment: a retrospective cohort study.术前治疗的胃癌患者中全身炎症标志物和三级淋巴结构与病理完全缓解的相关性:一项回顾性队列研究。
Int J Surg. 2023 Dec 1;109(12):4151-4161. doi: 10.1097/JS9.0000000000000741.
8
Bruceine D and Narclasine inhibit the proliferation of breast cancer cells and the prediction of potential drug targets.布魯斯胺 D 和那可丁抑制乳腺癌細胞的增殖及潛在藥物靶點的預測。
PLoS One. 2024 Jan 12;19(1):e0297203. doi: 10.1371/journal.pone.0297203. eCollection 2024.
9
[Analysis of Salivary Microbiota Characteristics in Patients With Pulmonary Nodules: A Prospective Nonrandomized Concurrent Controlled Trial].[肺结节患者唾液微生物群特征分析:一项前瞻性非随机同期对照试验]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2023 Nov 20;54(6):1208-1218. doi: 10.12182/20231160103.
10
Cholesterol Metabolism in Pancreatic Cancer.胰腺癌中的胆固醇代谢
Cancers (Basel). 2023 Oct 27;15(21):5177. doi: 10.3390/cancers15215177.